These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

202 related items for PubMed ID: 8411069

  • 1. Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 3. Differential diagnosis and prognosis.
    Nicholson LV, Johnson MA, Bushby KM, Gardner-Medwin D, Curtis A, Ginjaar IB, den Dunnen JT, Welch JL, Butler TJ, Bakker E.
    J Med Genet; 1993 Sep; 30(9):745-51. PubMed ID: 8411069
    [Abstract] [Full Text] [Related]

  • 2. Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 2. Correlations within individual patients.
    Nicholson LV, Johnson MA, Bushby KM, Gardner-Medwin D, Curtis A, Ginjaar IB, den Dunnen JT, Welch JL, Butler TJ, Bakker E.
    J Med Genet; 1993 Sep; 30(9):737-44. PubMed ID: 8411068
    [Abstract] [Full Text] [Related]

  • 3. Integrated study of 100 patients with Xp21 linked muscular dystrophy using clinical, genetic, immunochemical, and histopathological data. Part 1. Trends across the clinical groups.
    Nicholson LV, Johnson MA, Bushby KM, Gardner-Medwin D, Curtis A, Ginjaar IB, den Dunnen JT, Welch JL, Butler TJ, Bakker E.
    J Med Genet; 1993 Sep; 30(9):728-36. PubMed ID: 8411067
    [Abstract] [Full Text] [Related]

  • 4.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 5. Is dystrophin always altered in Becker muscular dystrophy patients?
    Vainzof M, Passos-Bueno MR, Pavanello RC, Zatz M.
    J Neurol Sci; 1995 Jul; 131(1):99-104. PubMed ID: 7561956
    [Abstract] [Full Text] [Related]

  • 6. [Muscular dystrophies detected by immunophenotyping and genotype analysis (mRNA and DNA)].
    Lukás Z, Vojtísková M, Fajkusová L, Bednarík J, Kadanka Z, Hájek J, Hermanová M, Vohánka S, Vytopil M.
    Cesk Patol; 2001 Nov; 37(4):137-45. PubMed ID: 11813630
    [Abstract] [Full Text] [Related]

  • 7. Manifesting carriers of Xp21 muscular dystrophy; lack of correlation between dystrophin expression and clinical weakness.
    Sewry CA, Sansome A, Clerk A, Sherratt TG, Hasson N, Rodillo E, Heckmatt JZ, Strong PN, Dubowitz V.
    Neuromuscul Disord; 1993 Mar; 3(2):141-8. PubMed ID: 8358239
    [Abstract] [Full Text] [Related]

  • 8. Dystrophin analysis in the diagnosis of childhood muscular dystrophy: an immunohistochemical study of 75 cases.
    Jay V, Becker LE, Ackerley C, Ray P.
    Pediatr Pathol; 1993 Mar; 13(5):635-57. PubMed ID: 8247961
    [Abstract] [Full Text] [Related]

  • 9.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 10. Dystrophin in skeletal muscle. II. Immunoreactivity in patients with Xp21 muscular dystrophy.
    Nicholson LV, Davison K, Johnson MA, Slater CR, Young C, Bhattacharya S, Gardner-Medwin D, Harris JB.
    J Neurol Sci; 1989 Dec; 94(1-3):137-46. PubMed ID: 2693618
    [Abstract] [Full Text] [Related]

  • 11.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 12.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 13.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 14. Limb-girdle syndrome: a genetic study of 22 large Brazilian families. Comparison with X-linked Duchenne and Becker dystrophies.
    Passos-Bueno MR, Vainzof M, Pavanello Rde C, Pavanello-Filho I, Lima MA, Zatz M.
    J Neurol Sci; 1991 May; 103(1):65-75. PubMed ID: 1865235
    [Abstract] [Full Text] [Related]

  • 15.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 16.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 17.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. Quantitative and qualitative alterations of dystrophin are expressed in muscle cell cultures of Xp21 muscular dystrophy patients (Duchenne and Becker type).
    Mongini T, Doriguzzi C, Palmucci L, Chiadò-Piat L.
    Eur J Clin Invest; 1996 Apr; 26(4):322-4. PubMed ID: 8732491
    [Abstract] [Full Text] [Related]

  • 20. The "rescue" of dystrophin synthesis in boys with Duchenne muscular dystrophy.
    Nicholson LV.
    Neuromuscul Disord; 1993 Apr; 3(5-6):525-31. PubMed ID: 8186705
    [Abstract] [Full Text] [Related]

    Page: [Next] [New Search]
    of 11.